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Infection and Immunity, October 2000, p. 6041-6043, Vol. 68, No. 10
Department of Veterinary Pathology, Glasgow
University Veterinary School, Glasgow G61 1QH,1
and Vaccine Research Unit, Medeva, Department of Biochemistry,
Imperial College of Science, Technology, and Medicine, London SW7
2AZ,2 United Kingdom
Received 10 April 2000/Returned for modification 5 June
2000/Accepted 28 June 2000
We compared the ability of Salmonella enterica serovar
Typhimurium SL1344 aroA aroD (BRD509) and aroA
htrA (BRD807) mutants to act as live vectors for delivery of
fragment C of tetanus toxin (FrgC). FrgC was expressed in these strains
from either pTETnir15 or pTEThtrA1. BRD509FrgC+ strains
elicited ~2-log-higher serum anti-FrgC antibody titers than
BRD807FrgC+ strains. All mice immunized with
BRD807pTEThtrA1, BRD509pTEThtrA1, and BRD509pTETnir15 (but not
BRD807pTETnir15) were protected against tetanus.
0019-9567/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Comparison of Abilities of Salmonella
enterica Serovar Typhimurium aroA aroD and aroA
htrA Mutants To Act as Live Vectors

*
Corresponding author. Mailing address: Department of
Veterinary Pathology, Glasgow University Veterinary School, Bearsden Rd., Glasgow G61 1QH, United Kingdom. Phone: 0141-330-5780. Fax: 0141-330-5602. E-mail: M.Roberts{at}vet.gla.ac.uk.
Present address: Microscience, ICSM Hammersmith Campus, London, W12
0NN, United Kingdom.
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